Metabolic Activation of Proestrogens in the Environment by Cytochrome P450 System
Author:
Affiliation:
1. Nihon Pharmaceutical University
2. Graduate School of Biomedical Sciences, Hiroshima University
3. Research Institute for Radiation Biology and Medicine, Hiroshima University
Publisher
Pharmaceutical Society of Japan
Subject
Health, Toxicology and Mutagenesis,Toxicology
Link
http://www.jstage.jst.go.jp/article/jhs/54/4/54_4_343/_pdf
Reference91 articles.
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3. The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site
4. 4) Fang, H., Tong, W., Perkins, R., Soto, A. M., Prechtl, N. V. and Sheehan, D. M. (2000) Quantitative comparisons of in vitro assay for estrogenic activities. Environ. Health Perspect., 108, 723-729.
5. QSAR Models Using a Large Diverse Set of Estrogens
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